Canonical Allele Identifier: CA508304831

Gene: POLD1

Linked Data

• ClinVar Variation Id: 1758011
• ClinVar RCV Id: RCV002382586 ; RCV003776369
• dbSNP Id: rs757184235
• gnomAD v4: 19-50402341-G-T
• MyVariant Identifiers: chr19:g.50905598G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50402341G>T , CM000681.2:g.50402341G>T	GRCh38
NC_000019.9:g.50905598G>T , CM000681.1:g.50905598G>T	GRCh37
NC_000019.8:g.55597410G>T	NCBI36
NG_033800.1:g.23019G>T , LRG_785:g.23019G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000593887.2:c.726G>T	ENSP00000472607.2:p.Ala242=
ENST00000600746.2:n.917G>T
ENST00000644560.2:c.726G>T	ENSP00000495618.2:p.Ala242=
ENST00000687454.1:c.726G>T	ENSP00000510052.1:p.Ala242=
ENST00000440232.7:c.726G>T MANE Select	ENSP00000406046.1:p.Ala242=
ENST00000595904.6:c.726G>T	ENSP00000472445.1:p.Ala242=
ENST00000599857.7:c.726G>T	ENSP00000473052.1:p.Ala242=
ENST00000601098.6:c.726G>T	ENSP00000472600.2:p.Ala242=
ENST00000613923.6:c.726G>T	ENSP00000481858.2:p.Ala242=
ENST00000643407.1:c.726G>T	ENSP00000496078.1:p.Ala242=
ENST00000440232.6:c.726G>T	ENSP00000406046.1:p.Ala242=
ENST00000595904.5:c.726G>T	ENSP00000472445.1:p.Ala242=
ENST00000599857.5:c.726G>T	ENSP00000473052.1:p.Ala242=
ENST00000600746.1:n.831G>T
ENST00000600859.5:c.726G>T	ENSP00000470726.1:p.Ala242=
ENST00000613923.4:c.726G>T	ENSP00000481858.1:p.Ala242=
NM_001256849.1:c.726G>T , LRG_785t1:c.726G>T	NP_001243778.1:p.Ala242=
NM_001308632.1:c.726G>T , LRG_785t2:c.726G>T	NP_001295561.1:p.Ala242=
NM_002691.3:c.726G>T	NP_002682.2:p.Ala242=
NR_046402.1:n.795G>T
XM_005259008.3:c.726G>T	XP_005259065.1:p.Ala242=
XM_011527038.1:c.726G>T	XP_011525340.1:p.Ala242=
XM_011527039.1:c.726G>T	XP_011525341.1:p.Ala242=
XR_935835.1:n.828G>T
XM_005259008.4:c.726G>T	XP_005259065.1:p.Ala242=
XM_017026881.1:c.726G>T	XP_016882370.1:p.Ala242=
XM_017026882.2:c.726G>T	XP_016882371.1:p.Ala242=
XR_935835.2:n.827G>T
NM_002691.4:c.726G>T MANE Select	NP_002682.2:p.Ala242=
NR_046402.2:n.771G>T